Canonical Allele Identifier: PA2830263905
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 963725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Lys309Glu
CA398532989
NM_144997.7:c.925A>G